drugset / Trial / NCT03343639

Study of the Efficacy, Safety and Tolerability of Serlopitant for the Treatment of Pruritus (Itch) With Plaque Psoriasis

NCT03343639 ↗

Phase 2 Completed 204 enrolled Vyne Therapeutics Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Study of the efficacy, safety, and tolerability of serlopitant for the treatment of pruritus in adults with plaque psoriasis

Timeline

Start
2017-11-01
Primary completion
2018-10-23
Completion
2018-11-12

Outcome

Met primary endpoint

paper The WI-NRS 4-point response rate at 8 weeks (primary end point) was 33.3% for serlopitant vs 21.1% for placebo (P = .028); PMID 32007513 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Serlopitant Small molecule 5 mg Oral

Indications